Evidence map›Paper›PMID 32128257›Full record

ArticleNPJ vaccines2020

Modified mRNA/lipid nanoparticle-based vaccines expressing respiratory syncytial virus F protein variants are immunogenic and protective in rodent models of RSV infection.

Amy S Espeseth, Pedro J Cejas, Michael P Citron, Dai Wang, Daniel J DiStefano, Cheryl Callahan, Gregory O' Donnell, Jennifer D Galli, Ryan Swoyer, Sinoeun Touch and 15 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
15.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

117 citing papers in PubMed, 180 citations in OpenAlex.

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57 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 2 institutions in 1 country.

Amy S Espeseth1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Pedro J Cejas1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Michael P Citron1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Dai Wang1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.ORCID 0000-0001-5666-8622
Daniel J DiStefano1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Cheryl Callahan1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Gregory O' Donnell2Pharmacology, Merck & Co., Inc., Kenilworth, NJ USA.
Jennifer D Galli1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Ryan Swoyer1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Sinoeun Touch1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Zhiyun Wen1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Joseph Antonello3Biostatistics, Merck & Co., Inc., Kenilworth, NJ USA.
Lan Zhang1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Jessica A Flynn1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Kara S Cox1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Daniel C Freed1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Kalpit A Vora1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Kapil BahlModerna, Inc., Cambridge, MA USA.
Andrew H Latham5Pharmaceutical Science, Merck & Co., Inc., Kenilworth, NJ USA.
Jeffrey S Smith5Pharmaceutical Science, Merck & Co., Inc., Kenilworth, NJ USA.
Marian E Gindy5Pharmaceutical Science, Merck & Co., Inc., Kenilworth, NJ USA.
Giuseppe CiaramellaModerna, Inc., Cambridge, MA USA.ORCID 0000-0003-3339-7211
Daria Hazuda1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Christine A ShawModerna, Inc., Cambridge, MA USA.
Andrew J Bett1ID/Vaccines Discovery, Merck & Co., Inc., Kenilworth, NJ USA.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USModerna Therapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RSV Fusion (F) protein is a target for neutralizing antibody responses and is a focus for vaccine discovery; however, the process of RSV entry requires F to adopt a metastable prefusion form and transition to a more stable postfusion form, which displays less potent neutralizing epitopes. mRNA vaccines encode antigens that are translated by host cells following vaccination, which may allow conformational transitions similar to those observed during natural infection to occur. Here we evaluate a panel of chemically modified mRNA vaccines expressing different forms of the RSV F protein, including secreted, membrane associated, prefusion-stabilized, and non-stabilized structures, for conformation, immunogenicity, protection, and safety in rodent models. Vaccination with mRNA encoding native RSV F elicited antibody responses to both prefusion- and postfusion-specific epitopes, suggesting that this antigen may adopt both conformations in vivo. Incorporating prefusion stabilizing mutations further shifts the immune response toward prefusion-specific epitopes, but does not impact neutralizing antibody titer. mRNA vaccine candidates expressing either prefusion stabilized or native forms of RSV F protein elicit robust neutralizing antibody responses in both mice and cotton rats, similar to levels observed with a comparable dose of adjuvanted prefusion stabilized RSV F protein. In contrast to the protein subunit vaccine, mRNA-based vaccines elicited robust CD4+ and CD8+ T-cell responses in mice, highlighting a potential advantage of the technology for vaccines requiring a cellular immune response for efficacy.

Indexed as

RNA vaccinesVaccinesVirology

Identifiers

PMID32128257
PMCPMC7021756
OpenAlexW3005809864

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.